Allele Registry

Canonical Allele Identifier: PA2826632371

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131393

RCV000212673

RCV000630013

RCV001355155

RCV001818325

RCV003462013

RCV003998102

ClinVar Variation:

142327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268422.1:p.Arg674Cys	CA011096 NM_001281493.2:c.2020C>T